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Tatsuya Okuzumi
Observed names:
T. OKUZUMI,
奥住 竜哉,
竜哉 奥住
Institution:
Ajinomoto (Japan)
Observed institutions:
Tokyo Institute of Technology,
Howard Hughes Medical Institute,
University of California, San Francisco,
Ajinomoto (Japan)
ORCID:
0000-0001-5839-6958
Observed ORCID:
0000-0001-5839-6958
OpenAlex ID:
A5010724729
Inhibitor hijacking of Akt activation
2009
·
Tatsuya Okuzumi
, Dorothea Fiedler
, et al.
·
Nature Chemical Biology
·
302
Exo-Cleavable Linkers: Enhanced Stability and Therapeutic Efficacy in Antibody–Drug Conjugates
2024
·
Tomohiro Watanabe
, Naoko Arashida
, et al.
·
Journal of Medicinal Chemistry
·
73
AJICAP Second Generation: Improved Chemical Site-Specific Conjugation Technology for Antibody–Drug Conjugate Production
2023
·
Tomohiro Fujii
, Yutaka Matsuda
, et al.
·
Bioconjugate Chemistry
·
66
PDF
Chemical Site-Specific Conjugation Platform to Improve the Pharmacokinetics and Therapeutic Index of Antibody–Drug Conjugates
2021
·
Yutaka Matsuda
, Takuya Seki
, et al.
·
Molecular Pharmaceutics
·
64
A Purification Strategy Utilizing Hydrophobic Interaction Chromatography to Obtain Homogeneous Species from a Site-Specific Antibody Drug Conjugate Produced by AJICAP™ First Generation
2020
·
Yutaka Matsuda
, Monica Leung
, et al.
·
Antibodies
·
37
PDF
AJICAP-M: Traceless Affinity Peptide Mediated Conjugation Technology for Site-Selective Antibody–Drug Conjugate Synthesis
2024
·
Yutaka Matsuda
, Natsuki Shikida
, et al.
·
Organic Letters
·
30
PDF
Chromatographic analysis of site-specific antibody-drug conjugates produced by AJICAP first-generation technology using a recombinant FcγIIIa receptor-ligand affinity column
2021
·
Yutaka Matsuda
, Atis Chakrabarti
, et al.
·
Journal of Chromatography B
·
28
Gram-Scale Antibody–Drug Conjugate Synthesis by Site-Specific Chemical Conjugation: AJICAP First Generation
2019
·
Yutaka Matsuda
, Kei Yamada
, et al.
·
Organic Process Research & Development
·
28
Synthesis and evaluation of indazole based analog sensitive Akt inhibitors
2010
·
Tatsuya Okuzumi
, Gregory S Ducker
, et al.
·
Molecular BioSystems
·
20
Efficient Solid-Phase Synthesis of Diverse 2-Aminoquinazolin-4-ones from Resin-Bound Anilines
2003
·
Shingo Makino
, Tatsuya Okuzumi
, et al.
·
Journal of Combinatorial Chemistry
·
18
Efficient solid-phase synthesis of quinazoline-2,4-diones with various substituents on aromatic rings
2003
·
Tatsuya Okuzumi
, Eiji Nakanishi
, et al.
·
Tetrahedron
·
17
Efficient solid-phase synthesis of diverse 1,2,3-benzotriazin-4-ones using tert-butyl nitrite
2003
·
Tatsuya Okuzumi
, Eiji Nakanishi
, et al.
·
Tetrahedron Letters
·
15
Stereochemistry of the reduction of 24-ethyldesmosterol to sitosterol in tissue cultures of Oryza sativa
1998
·
Yoshinori Fujimoto
, Naoko Sato
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
11
Biological Evaluation of Maytansinoid-Based Site-Specific Antibody-Drug Conjugate Produced by Fully Chemical Conjugation Approach: AJICAP®
2022
·
Takuya Seki
, Kei Yamada
, et al.
·
Frontiers in Bioscience-Landmark
·
10
PDF
Solid-phase synthesis of 2-substituted-3-(substituted sulfanyl)-1,2,4-benzothiadiazine 1,1-dioxide library
2002
·
Shingo Makino
, Tatsuya Okuzumi
, et al.
·
Tetrahedron Letters
·
10
Mechanism of the double bond isomerization from Δ24(28) to Δ24(25) in sitosterol biosynthesis in higher plants
1999
·
Tatsuya Okuzumi
, Noriyuki Hara
, et al.
·
Tetrahedron Letters
·
10
Mechanism of the second methylation in sitosterol side-chain biosynthesis in higher plants: metabolic fate of 28-hydrogens of 24-methylenecholesterol in Morus alba cell cultures
2000
·
Tatsuya Okuzumi
, Yuko Kaji
, et al.
·
Tetrahedron Letters
·
7
AJICAP®: Chemical site-specific conjugation technology for next-generation ADC
2021
·
Tatsuya Okuzumi
·
The Chemical Society of Japan
AJICAP™: Development of a Chemical Site-Specific Conjugation Technology for Antibody-Drug Conjugates
2020
·
Kei Yamada
, Tatsuya Okuzumi
·
Journal of Synthetic Organic Chemistry Japan
分科会bグループ発表会 技術マネジメント/技術の体系化 (特集 研究・技術人材の育成) -- (企業研究会 第11期 研究・技術人材開発フォーラム)
2015
·
伸一郎 川上
, 竜哉 奥住
, et al.
·
BuR - Business Research
医薬品産業の過去・現在・未来
2014
·
奥住 竜哉
·
ファルマシア
平賀源内に学ぶイノベーターになる方法, 出川通著, 言視舎, 四六判, 207頁, 1,575円
2013
·
竜哉 奥住
·
ファルマシア
遺伝子医学mook21号 最新ペプチド合成技術とその創薬研究への応用, 木曽良明編, 向井秀仁編集協力, メディカルドゥ, B5, 316頁, 5,600円
2012
·
竜哉 奥住
·
ファルマシア
73(p-57) 植物ステロール側鎖生合成機構の解析 : C-28位における反応の立体化学(ポスター発表の部)
2002
·
竜哉 奥住
, 武史 小網
, et al.
·
天然有機化合物討論会講演要旨集
ChemInform Abstract: Stereochemistry of the Reduction of 24‐Ethyldesmosterol to Sitosterol in Tissue Cultures of Oryza sativa.
1998
·
Y. FUJIMOTO
, N. SATO
, et al.
·
ChemInform
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Works count:
25
Citation count:
746
H-index:
12
I10-index:
16
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